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VeriCheck Drug Test Dip

Verify Diagnostics Inc · Model 1.0 · UDI-DI 00870266001055

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10
510(k) clearances
8
Adverse events
0
Recalls
52
Facilities

Description

MET1000

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.